Back Article

Kim YJ, Zhang D. 2018. Molecular control of male fertility for crop hybrid breeding. Trends in Plant Science 23:53−65

Gómez JF, Talle B, Wilson ZA. 2015. Anther and pollen development: a conserved developmental pathway. Journal of Integrative Plant Biology 57:876−91

Åstrand J, Knight C, Robson J, Talle B, Wilson ZA. 2021. Evolution and diversity of the angiosperm anther: trends in function and development. Plant Reproduction 34:307−19

Marchant DB, Walbot V. 2022. Anther development—the long road to making pollen. The Plant Cell 34:4677−95

Wan X, Wu S, Li Z, An X, Tian Y. 2020. Lipid metabolism: critical roles in male fertility and other aspects of reproductive development in plants. Molecular Plant 13:955−83

Lee SK, Lee J, Jo M, Jeon JS. 2022. Exploration of sugar and starch metabolic pathway crucial for pollen fertility in rice. International Journal of Molecular Sciences 23:14091

Zhang D, Shi J, Yang X. 2016. Role of lipid metabolism in plant pollen exine development. In Lipids in Plant and Algae Development. Subcellular Biochemistry, eds. Nakamura Y, Li-Beisson Y. vol 86. Cham, Switzerland: Springer, Cham. pp. 315–37. https://doi.org/10.1007/978-3-319-25979-6_13

Shi J, Cui M, Yang L, Kim YJ, Zhang D. 2015. Genetic and biochemical mechanisms of pollen wall development. Trends in Plant Science 20:741−53

Zhang D, Luo X, Zhu L. 2011. Cytological analysis and genetic control of rice anther development. Journal of Genetics and Genomics 38:379−90

Wilson ZA, Zhang D. 2009. From Arabidopsis to rice: pathways in pollen development. Journal of Experimental Botany 60:1479−92

Ma X, Wu Y, Zhang G. 2021. Formation pattern and regulatory mechanisms of pollen wall in Arabidopsis. Journal of Plant Physiology 260:153388

Sun Y, Fu M, Ang Y, Zhu L, Wei L, et al. 2022. Combined analysis of transcriptome and metabolome reveals that sugar, lipid, and phenylpropane metabolism are essential for male fertility in temperature-induced male sterile rice. Frontiers in Plant Science 13:945105

Fang Y, Yang J, Guo X, Qin Y, Zhou H, et al. 2022. CRISPR/Cas9-induced mutagenesis of TMS5 confers thermosensitive genic male sterility by influencing protein expression in rice (Oryza sativa L.). International Journal of Molecular Sciences 23:8354

Abbas A, Yu P, Sun L, Yang Z, Chen D, et al. 2021. Exploiting genic male sterility in rice: from molecular dissection to breeding applications. Frontiers in Plant Science 12:629314

Sze H, Palanivelu R, Harper JF, Johnson MA. 2021. Holistic insights from pollen omics: co-opting stress-responsive genes and ER-mediated proteostasis for male fertility. Plant Physiology 187:2361−80

Tang H, Song Y, Guo J, Wang J, Zhang L, et al. 2018. Physiological and metabolome changes during anther development in wheat (Triticum aestivum L.). Plant Physiology and Biochemistry 132:18−32

Li C, Tao R, Li Y, Duan M, Xu J. 2020. Transcriptome analysis of the thermosensitive genic male-sterile line provides new insights into fertility alteration in rice (Oryza sativa). Genomics 112:2119−29

Sun S, Wang D, Li J, Lei Y, Li G, et al. 2021. Transcriptome analysis reveals photoperiod-associated genes expressed in rice anthers. Frontiers in Plant Science 12:621561

Yu J, Han J, Kim Y-J, Song M, Yang Z, et al. 2017. Two rice receptor-like kinases maintain male fertility under changing temperatures. Proceedings of the National Academy of Sciences 114:12327−32

Jin J, Gui S, Li Q, Wang Y, Zhang H, et al. 2020. The transcription factor GATA10 regulates fertility conversion of a two-line hybrid tms5 mutant rice via the modulation of Ub _L40 expression. Journal of Integrative Plant Biology 62:1034−56

Wen J, Wang L, Wang J, Zeng Y, Xu Y, et al. 2019. The transcription factor OsbHLH138 regulates thermosensitive genic male sterility in rice via activation of TMS5. Theoretical and Applied Genetics 132:1721−32

Zhou H, Zhou M, Yang Y, Li J, Zhu L, et al. 2014. RNase Z^S1 processes Ub _L40 mRNAs and controls thermosensitive genic male sterility in rice. Nature Communications 5:4884

Zhang H, Liang W, Yang X, Luo X, Jiang N, et al. 2010. Carbon Starved Anther encodes a MYB domain protein that regulates sugar partitioning required for rice pollen development. The Plant Cell 22:672−89

Zhang H, Xu C, He Y, Zong J, Yang X, et al. 2013. Mutation in CSA creates a new photoperiod-sensitive genic male sterile line applicable for hybrid rice seed production. Proceedings of the National Academy of Sciences 110:76−81

Li J, Wang D, Sun S, Sun L, Zong J, et al. 2022. The regulatory role of Carbon Starved Anther-mediated photoperiod-dependent male fertility in rice. Plant Physiology 189:955−71

Wang D, Li J, Sun L, Hu Y, Yu J, et al. 2021. Two rice MYB transcription factors maintain male fertility in response to photoperiod by modulating sugar partitioning. New Phytologist 231:1612−29

Chen R, Zhao X, Shao Z, Wei Z, Wang Y, et al. 2007. Rice UDP-Glucose Pyrophosphorylase1 is essential for pollen callose deposition and its cosuppression results in a new type of thermosensitive genic male sterility. The Plant Cell 19:847−61

Virmani SS, Ilyas-Ahmed M. 2001. Environment-sensitive genic male sterility (EGMS) in crops. In Advances in Agronomy. vol 72. Amsterdam: Elsevier. pp. 139–95

Fan Y, Yang J, Mathioni SM, Yu J, Shen J, et al. 2016. PMS1T, producing phased small-interfering RNAs, regulates photoperiod-sensitive male sterility in rice. PNAS 113:15144−49

Ding J, Shen J, Mao H, Xie W, Li X, et al. 2012. RNA-directed DNA methylation is involved in regulating photoperiod-sensitive male sterility in rice. Molecular Plant 5:1210−16

Lu Q, Li X, Guo D, Xu C, Zhang Q. 2005. Localization of pms3, a gene for photoperiod-sensitive genic male sterility, to a 28.4-kb DNA fragment. Molecular Genetics and Genomics 273:507−11

Chen H, Zhang Z, Ni E, Lin J, Peng G, et al. 2020. HMS1 interacts with HMS1I to regulate very-long-chain fatty acid biosynthesis and the humidity-sensitive genic male sterility in rice (Oryza sativa). New Phytologist 225:2077−93

Shi Q, Lou Y, Shen S, Wang S, Zhou L, et al. 2021. A cellular mechanism underlying the restoration of thermo/photoperiod-sensitive genic male sterility. Molecular Plant 14:2104−14

Wang K, Yu Y, Jia X, Zhou S, Zhang F, et al. 2022. Delayed callose degradation restores the fertility of multiple P/TGMS lines in Arabidopsis. Journal of Integrative Plant Biology 64:717−30

Zhang C, Ren M, Han W, Zhang Y, Huang M, et al. 2022. Slow development allows redundant genes to restore the fertility of rpg1, a TGMS line in Arabidopsis. The Plant Journal 109:1375−85

Zhang C, Xu T, Ren M, Zhu J, Shi Q, et al. 2020. Slow development restores the fertility of photoperiod-sensitive male-sterile plant lines. Plant Physiology 184:923−32

Xu X, Qian X, Wang K, Yu Y, Guo Y, et al. 2021. Slowing development facilitates Arabidopsis mgt mutants to accumulate enough magnesium for pollen formation and fertility restoration. Frontiers in Plant Science 11:621338

Zhu J, Lou Y, Shi Q, Zhang S, Zhou W, et al. 2020. Slowing development restores the fertility of thermo-sensitive male-sterile plant lines. Nature Plants 6:360−67

Cui Y, Lu X, Gou X. 2022. Receptor-like protein kinases in plant reproduction: Current understanding and future perspectives. Plant Communications 3:100273

Cai W, Zhang D. 2018. The role of receptor-like kinases in regulating plant male reproduction. Plant Reproduction 31:77−87

Soltabayeva A, Dauletova N, Serik S, Sandybek M, Omondi JO, et al. 2022. Receptor-like kinases (LRR-RLKs) in response of plants to biotic and abiotic stresses. Plants 11:2660

Hu C, Zhu Y, Cui Y, Cheng K, Liang W, et al. 2018. A group of receptor kinases are essential for CLAVATA signalling to maintain stem cell homeostasis. Nature Plants 4:205−11

Yang L, Qian X, Chen M, Fei Q, Meyers BC, et al. 2016. Regulatory role of a receptor-like kinase in specifying anther cell identity. Plant Physiology 171:2085−100

Han Y, Jiang S, Zhong X, Chen X, Ma C, et al. 2023. Low temperature compensates for defective tapetum initiation to restore the fertility of the novel TGMS line ostms15. Plant Biotechnology Journal 21:1659−70

Bhogireddy S, Mangrauthia SK, Kumar R, Pandey AK, Singh S, et al. 2021. Regulatory non-coding RNAs: a new frontier in regulation of plant biology. Functional & Integrative Genomics 21:313−30

Quan M, Chen J, Zhang D. 2015. Exploring the secrets of long noncoding RNAs. International Journal of Molecular Sciences 16:5467−96

Dziegielewski W, Ziolkowski PA. 2021. License to regulate: noncoding RNA special agents in plant meiosis and reproduction. Frontiers in Plant Science 12:662185

Chen L, Liu Y. 2014. Male sterility and fertility restoration in crops. Annual Review of Plant Biology 65:579−606

Fan Y, Zhang Q. 2018. Genetic and molecular characterization of photoperiod and thermo-sensitive male sterility in rice. Plant Reproduction 31:3−14

Peng G, Liu Z, Zhuang C, Zhou H. 2023. Environment-sensitive genic male sterility in rice and other plants. Plant, Cell & Environment 46:1120−42

Ding J, Lu Q, Ouyang Y, Mao H, Zhang P, et al. 2012. A long noncoding RNA regulates photoperiod-sensitive male sterility, an essential component of hybrid rice. PNAS 109:2654−59

Zhou H, Liu Q, Li J, Jiang D, Zhou L, et al. 2012. Photoperiod- and thermo-sensitive genic male sterility in rice are caused by a point mutation in a novel noncoding RNA that produces a small RNA. Cell Research 22:649−60

Si F, Luo H, Yang C, Gong J, Yan B, et al. 2023. Mobile ARGONAUTE 1d binds 22-nt miRNAs to generate phasiRNAs important for low-temperature male fertility in rice. Science China Life Sciences 66:197−208

Shi C, Zhang J, Wu B, Jouni R, Yu C, et al. 2022. Temperature-sensitive male sterility in rice determined by the roles of AGO1d in reproductive phasiRNA biogenesis and function. New Phytologist 236:1529−44

Lee YS, Maple R, Dürr J, Dawson A, Tamim S, et al. 2021. A transposon surveillance mechanism that safeguards plant male fertility during stress. Nature Plants 7:34−41

Teng C, Zhang H, Hammond R, Huang K, Meyers BC, et al. 2020. Dicer-like 5 deficiency confers temperature-sensitive male sterility in maize. Nature Communications 11:2912

Canino G, Bocian E, Echeverría N, Echeverría M, Forner J, et al. 2009. Arabidopsis encodes four tRNase Z enzymes. Plant Physiology 150:1494−502

Vogel A, Schilling O, Späth B, Marchfelder A. 2005. The tRNase Z family of proteins: physiological functions, substrate specificity and structural properties. Biological Chemistry 386:1253−64

Cartalas J, Coudray L, Gobert A. 2022. How RNases shape mitochondrial transcriptomes. International Journal of Molecular Sciences 23:6141

Wen J, Zeng Y, Chen Y, Fan F, Li S. 2021. Genic male sterility increases rice drought tolerance. Plant Science 312:111057

Verma N. 2019. Transcriptional regulation of anther development in Arabidopsis. Gene 689:202−9

Millar AA, Gubler F. 2005. The Arabidopsis GAMYB-Like genes, MYB33 and MYB65, are microrna-regulated genes that redundantly facilitate anther development. The Plant Cell 17:705−21

Wu L, Jing X, Zhang B, Chen S, Xu R, et al. 2022. A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility. Nature Communications 13:2055

Hou J, Fan W, Ma R, Li B, Yuan Z, et al. 2022. MALE STERILITY 3 encodes a plant homeodomain-finger protein for male fertility in soybean. Journal of Integrative Plant Biology 64:1076−86

Liu Z, Bao W, Liang W, Yin J, Zhang D. 2010. Identification of gamyb-4 and analysis of the regulatory role of GAMYB in rice anther development. Journal of Integrative Plant Biology 52:670−78

Alonso-Peral MM, Li J, Li Y, Allen RS, Schnippenkoetter W, et al. 2010. The microRNA159-regulated GAMYB-like genes inhibit growth and promote programmed cell death in arabidopsis. Plant Physiology 154:757−71

Kaneko M, Inukai Y, Ueguchi-Tanaka M, Itoh H, Izawa T, et al. 2004. Loss-of-function mutations of the rice GAMYB gene impair α-amylase expression in aleurone and flower development. The Plant Cell 16:33−44

Wang TY, Wang YX, You CJ. 2021. Structural and functional characteristics of plant PHD domain-containing proteins. Hereditas 43:323−39

Sanchez R, Zhou M-M. 2011. The PHD finger: a versatile epigenome reader. Trends in Biochemical Sciences 36:364−72

Plevin MJ, Mills MM, Ikura M. 2005. The LxxLL motif: a multifunctional binding sequence in transcriptional regulation. Trends in Biochemical Sciences 30:66−69

Niu N, Liang W, Yang X, Jin W, Wilson ZA, et al. 2013. EAT1 promotes tapetal cell death by regulating aspartic proteases during male reproductive development in rice. Nature Communications 4:1445

Tang J, Tian X, Mei E, He M, Gao J, et al. 2022. WRKY53 negatively regulates rice cold tolerance at the booting stage by fine-tuning anther gibberellin levels. The Plant Cell 34:4495−515

Zhang D-S, Liang W-Q, Yuan Z, Li N, Shi J, et al. 2008. Tapetum Degeneration Retardation is critical for aliphatic metabolism and gene regulation during rice pollen development. Molecular Plant 1:599−610

Li N, Zhang DS, Liu HS, Yin CS, Li X, et al. 2006. The Rice Tapetum Degeneration Retardation gene is required for tapetum degradation and anther development. The Plant Cell 18:2999−3014

Li H, Yuan Z, Vizcay-Barrena G, Yang C, Liang W, et al. 2011. PERSISTENT TAPETAL CELL1 encodes a PHD-finger protein that is required for tapetal cell death and pollen development in rice. Plant Physiology 156:615−30

Yang Z, Liu L, Sun L, Yu P, Zhang P, et al. 2019. OsMS1 functions as a transcriptional activator to regulate programmed tapetum development and pollen exine formation in rice. Plant Molecular Biology 99:175−91

Ito T, Nagata N, Yoshiba Y, Ohme-Takagi M, Ma H, et al. 2007. Arabidopsis MALE STERILITY1 encodes a PHD-type transcription factor and regulates pollen and tapetum development. The Plant Cell 19:3549−62

Fernández Gómez J, Wilson ZA. 2014. A barley PHD finger transcription factor that confers male sterility by affecting tapetal development. Plant Biotechnology Journal 12:765−77

Zhang D, Wu S, An X, Xie K, Dong Z, et al. 2018. Construction of a multicontrol sterility system for a maize male-sterile line and hybrid seed production based on the ZmMs7 gene encoding a PHD-finger transcription factor. Plant Biotechnology Journal 16:459−71

An X, Ma B, Duan M, Dong Z, Liu R, et al. 2020. Molecular regulation of ZmMs7 required for maize male fertility and development of a dominant male-sterility system in multiple species. PNAS 117:23499−509

Xue Z, Xu X, Zhou Y, Wang X, Zhang Y, et al. 2018. Deficiency of a triterpene pathway results in humidity-sensitive genic male sterility in rice. Nature Communications 9:604

Aarts MG, Keijzer CJ, Stiekema WJ, Pereira A. 1995. Molecular characterization of the CER1 gene of arabidopsis involved in epicuticular wax biosynthesis and pollen fertility. The Plant Cell 7:2115−27

Zhan H, Xiong H, Wang S, Yang Z-N. 2018. Anther endothecium-derived very-long-chain fatty acids facilitate pollen hydration in arabidopsis. Molecular Plant 11:1101−4

Xu F, Zheng L, Yang Z, Zhang S. 2020. Arabidopsis ECERIFERUM3 (CER3) functions to maintain hydration for pollen–stigma recognition during fertilization. Journal of Plant Biology 63:347−59

Ariizumi T, Hatakeyama K, Hinata K, Sato S, Kato T, et al. 2003. A novel male-sterile mutant of Arabidopsis thaliana,faceless pollen-1, produces pollen with a smooth surface and an acetolysis-sensitive exine. Plant Molecular Biology 53:107−16

Chen X, Goodwin SM, Boroff VL, Liu X, Jenks MA. 2003. Cloning and characterization of the WAX2 gene of Arabidopsis involved in cuticle membrane and wax production. The Plant Cell 15:1170−85

Bernard A, Domergue F, Pascal S, Jetter R, Renne C, et al. 2012. Reconstitution of plant alkane biosynthesis in yeast demonstrates that Arabidopsis ECERIFERUM1 and ECERIFERUM3 are core components of a very-long-chain alkane synthesis complex. The Plant Cell 24:3106−18

Preuss D, Lemieux B, Yen G, Davis RW. 1993. A conditional sterile mutation eliminates surface components from Arabidopsis pollen and disrupts cell signaling during fertilization. Genes & Development 7:974−85

Fiebig A, Mayfield JA, Miley NL, Chau S, Fischer RL, et al. 2000. Alterations in CER6, a gene identical to CUT1, differentially affect long-chain lipid content on the surface of pollen and stems. The Plant Cell 12:2001−8

Jessen D, Olbrich A, Knüfer J, Krüger A, Hoppert M, et al. 2011. Combined activity of LACS1 and LACS4 is required for proper pollen coat formation in Arabidopsis. The Plant Journal 68:715−26

Ni E, Deng L, Chen H, Lin J, Ruan J, et al. 2021. OsCER1 regulates humidity-sensitive genic male sterility through very-long-chain (VLC) alkane metabolism of tryphine in rice. Functional Plant Biology 48:461

Ni E, Zhou L, Li J, Jiang D, Wang Z, et al. 2018. OsCER1 plays a pivotal role in very-long-chain alkane biosynthesis and affects plastid development and programmed cell death of tapetum in rice (Oryza sativa L.). Frontiers in Plant Science 9:1217

Yu B, Liu L, Wang T. 2019. Deficiency of very long chain alkanes biosynthesis causes humidity-sensitive male sterility via affecting pollen adhesion and hydration in rice. Plant, Cell & Environment 42:3340−54

Wang X, Guan Y, Zhang D, Dong X, Tian L, et al. 2017. A β-Ketoacyl-CoA synthase is involved in rice leaf cuticular wax synthesis and requires a CER2-LIKE protein as a cofactor. Plant Physiology 173:944−55

Zheng H, Rowland O, Kunst L. 2005. Disruptions of the Arabidopsis Enoyl-CoA reductase gene reveal an essential role for very-long-chain fatty acid synthesis in cell expansion during plant morphogenesis. The Plant Cell 17:1467−81

Ashraf MF, Peng G, Liu Z, Noman A, Alamri S, et al. 2020. Molecular control and application of male fertility for two-line hybrid rice breeding. International Journal of Molecular Sciences 21:7868

Zhang Y, Li Y, Zhong X, Wang J, Zhou L, et al. 2022. Mutation of glucose-methanol-choline oxidoreductase leads to thermosensitive genic male sterility in rice and Arabidopsis. Plant Biotechnology Journal 20:2023−35

Xu L, Tang Y, Yang Y, Wang D, Wang H, et al. 2023. Microspore-expressed SCULP1 is required for p-coumaroylation of sporopollenin, exine integrity, and pollen development in wheat. New Phytologist 239:102−15

Schuhmann P, Engstler C, Klöpfer K, Gügel IL, Abbadi A, et al. 2022. Two wrongs make a right: heat stress reversion of a male-sterile Brassica napus line. Journal of Experimental Botany 73:3531−51

Zhao Z, Wang C, Yu X, Tian Y, Wang W, et al. 2022. Auxin regulates source-sink carbohydrate partitioning and reproductive organ development in rice. PNAS 119:e2121671119

Jin Y, Song X, Chang H, Zhao Y, Cao C, et al. 2022. The GA–DELLA–OsMS188 module controls male reproductive development in rice. New Phytologist 233:2629−42

Zhang J, Zong X, Yu G, Li J, Zhang W. 2006. Relationship between phytohormones and male sterility in thermo-photo-sensitive genic male sterile (TGMS) Wheat. Euphytica 150:241−48

He Y, Liu C, Zhu L, Fu M, Sun Y, et al. 2021. Jasmonic acid plays a pivotal role in pollen development and fertility regulation in different types of P(T)GMS rice lines. International Journal of Molecular Sciences 22:7926

Yang Q, Nong X, Xu J, Huang F, Wang F, et al. 2021. Unraveling the genetic basis of fertility restoration for cytoplasmic male sterile line WNJ01A originated from Brassica juncea in Brassica napus. Frontiers in Plant Science 12:721980

Jin ZY, Zhe T, Jun CH, You J. 1996. Relationship between male fertility and endogenous phytohormones in photoperiod sensitive genic male sterile rice. Journal of Integrative Plant Biology 38:936−41

Fuglie K. 2021. Climate change upsets agriculture. Nature Climate Change 11:294−95

Dubey PK, Singh GS, Abhilash PC. 2016. Agriculture in a changing climate. Journal of Cleaner Production 113:1046−47

Shi J, An G, Weber APM, Zhang D. 2023. Prospects for rice in 2050. Plant, Cell & Environment 46:1037−45

Huang X, Han B. 2014. Natural variations and genome-wide association studies in crop plants. Annual Review of Plant Biology 65:531−51

Fernie AR, Yan J. 2019. De novo domestication: an alternative route toward new crops for the future. Molecular Plant 12:615−31

Sun M, Huang X, Yang J, Guan Y, Yang Z. 2013. Arabidopsis RPG1 is important for primexine deposition and functions redundantly with RPG2 for plant fertility at the late reproductive stage. Plant Reproduction 26:83−91

Guan Y, Huang X, Zhu J, Gao J, Zhang H, et al. 2008. RUPTURED POLLEN GRAIN1, a member of the MtN3/saliva gene family, is crucial for exine pattern formation and cell integrity of microspores in Arabidopsis. Plant Physiology 147:852−63

Ma Z, Leng Y, Chen G, Zhou P, Ye D, et al. 2015. The THERMOSENSITIVE MALE STERILE 1 interacts with the BiPs via DnaJ domain and stimulates their ATPase enzyme activities in Arabidopsis. PLoS One 10:e0132500

Yang K, Xia C, Liu X, Dou X, Wang W, et al. 2009. A mutation in THERMOSENSITIVE MALE STERILE 1, encoding a heat shock protein with DnaJ and PDI domains, leads to thermosensitive gametophytic male sterility in Arabidopsis. The Plant Journal 57:870−82

Deng Y, Srivastava R, Quilichini TD, Dong H, Bao Y, et al. 2016. IRE1, a component of the unfolded protein response signaling pathway, protects pollen development in Arabidopsis from heat stress. The Plant Journal 88:193−204

Mitterreiter MJ, Bosch FA, Brylok T, Schwenkert S. 2020. The ER luminal C-terminus of AtSec62 is critical for male fertility and plant growth in Arabidopsis thaliana. The Plant Journal 101:5−17

Mou Z, Wang X, Fu Z, Dai Y, Han C, et al. 2002. Silencing of phosphoethanolamine N-methyltransferase results in temperature-sensitive male sterility and salt hypersensitivity in Arabidopsis. The Plant Cell 14:2031−43

Wang H, Lu Y, Jiang T, Berg H, Li C, et al. 2013. The Arabidopsis U-box/ARM repeat E3 ligase AtPUB4 influences growth and degeneration of tapetal cells, and its mutation leads to conditional male sterility. The Plant Journal 74:511−23

Huang H, Wang C, Tian H, Sun Y, Xie D, et al. 2014. Amino acid substitutions of GLY98, LEU245 and GLU543 in COI1 distinctively affect jasmonate-regulated male fertility in Arabidopsis. Science China Life Sciences 57:145−54

Wei D, Liu M, Chen H, Zheng Y, Liu Y, et al. 2018. INDUCER OF CBF EXPRESSION 1 is a male fertility regulator impacting anther dehydration in Arabidopsis. PLoS Genetics 14:e1007695

Ishiguro S, Nishimori Y, Yamada M, Saito H, Suzuki T, et al. 2010. The Arabidopsis FLAKY POLLEN1 gene encodes a 3-Hydroxy-3-Methylglutaryl-coenzyme a synthase required for development of tapetum-specific organelles and fertility of pollen grains. Plant and Cell Physiology 51:896−911

Wang Y, Zha X, Zhang S, Qian X, Dong X, et al. 2010. Down-regulation of the OsPDCD5 gene induced photoperiod-sensitive male sterility in rice. Plant Science 178:221−28

Jiang S, Cai M, Ramachandran S. 2007. ORYZA SATIVA MYOSIN XI B controls pollen development by photoperiod-sensitive protein localizations. Developmental Biology 304:579−92

Chueasiri C, Chunthong K, Pitnjam K, Chakhonkaen S, Sangarwut N, et al. 2014. Rice ORMDL controls sphingolipid homeostasis affecting fertility resulting from abnormal pollen development. PLoS One 9:e106386

Yan W, Yuan S, Zu Y, Chang Z, Li Y, et al. 2023. Ornithine δ-aminotransferase OsOAT is critical for male fertility and cold tolerance during rice plant development. The Plant Journal 14(6):1301−18

Lin S, Liu Z, Sun S, Xue F, Li H, et al. 2023. Rice HEAT SHOCK PROTEIN60-3B maintains male fertility under high temperature by starch granule biogenesis. Plant Physiology 192:2301−17

Li J, Zhang H, Si X, Tian Y, Chen K, et al. 2017. Generation of thermosensitive male-sterile maize by targeted knockout of the ZmTMS5 gene. Journal of Genetics and Genomics 44:465−68

Huang W, Li Y, Du Y, Pan L, Huang Y, et al. 2022. Maize cytosolic invertase INVAN6 ensures faithful meiotic progression under heat stress. New Phytologist 236:2172−88

Fernández-Gómez J, Talle B, Wilson ZA. 2020. Increased expression of the MALE STERILITY1 transcription factor gene results in temperature-sensitive male sterility in barley. Journal of Experimental Botany 71:6328−39